Solutions · 02
Specialty-level panels for the clinics that need them.
Oncology, cardiology, neurology, and rare disease centers map polymorphic risk and pharmacogenomic profiles against deep phenotypic data.
Specialty-level panels with deep phenotypic integration.
Oncology
Polygenic risk scores for the most prevalent cancers, hereditary cancer carrier panels, and pharmacogenomic profiles relevant to oncology pharmacotherapy.
Cardiology
Cardiovascular polygenic risk modeling including coronary artery disease, atrial fibrillation, and heart failure cohorts, with antithrombotic-relevant PGx.
Neurology
Neurodegenerative risk modeling (Alzheimer’s, Parkinson’s) and pharmacogenomic decision-support across neuropsychiatric therapies.
Rare disease centers
Carrier status reports covering 40+ inherited conditions, supported by clinical-grade short-read sequencing and rigorous variant annotation.
Pharmacogenomics across specialties
100+ medications across 15+ drug classes, with actionable dosing and alternative-medication guidance at the point of care.
Rapid clinical reporting
Reports structured for clinician review with prioritized findings, evidence linkage, and patient-facing translation material.